No super-duper protocol in general (sorry), but I had a lot of problems with SYBR Green to start with. In general, I followed the ABgene protocol. Also, watch your primer concentrations and starting cncetration of cDNA or DNA. They are both key in generating good amplicons in SYBR green analysis.
http://www.abgene.com/productDetails.asp?prodID=31 there are some good data sheets here to download and potentially provide better real time results
hope it's of some help
G